Pulveroboletus ravenelii

Pulveroboletus ravenelii
Scientific classification
Kingdom: Fungi
Division: Basidiomycota
Class: Agaricomycetes
Order: Boletales
Family: Boletaceae
Genus: Pulveroboletus
Species: P. ravenelii
Binomial name
Pulveroboletus ravenelii
(Berk. & M.A.Curtis) Murrill (1909)
Synonyms[1]
  • Boletus ravenelii Berk. & M.A.Curtis (1853)
Pulveroboletus ravenelii
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Mycological characteristics

pores on hymenium

cap is convex

or flat
hymenium attachment is not applicable
stipe has a ring
spore print is olive-brown
ecology is mycorrhizal
edibility: edible

Pulveroboletus ravenelii, commonly known as Ravenel's bolete or the powdery sulfur bolete, is a species of bolete fungus in the family Boletaceae. Described as new to science in 1853, the widely distributed species is known from Asia, Australia, North America, Central America, and South America. Mycorrhizal with oak, the fungus fruits on the ground singly, scattered, or in groups in woods. Fruit bodies (mushrooms) have convex to flat, yellowish to brownish-red caps up to 10 cm (4 in) in diameter. On the cap underside, the pore surface is bright yellow before turning dingy yellow to grayish brown with age; it stains greenish blue then grayish brown after injury. A cottony and powdery partial veil remains as a ring on the stipe. The mushrooms are edible, and have been used in traditional Chinese medicine and for mushroom dyeing.

Taxonomy

The species was first described as Boletus ravenelii by Miles Joseph Berkeley and Moses Ashley Curtis in 1853. Specimens were sent to them by American botanist Henry William Ravenel, who collected them in South Carolina. They considered the bolete "a most splendid species closely allied to B. hemichrysus, and, like that, remarkable for the pulverulent veil."[2] The specific epithet honors Ravenel.[3] William Alphonso Murrill transferred the fungus to the genus Pulveroboletus in 1909, giving it the name by which it is known today.[4] The mushroom is commonly known as "Ravenel's bolete"[5] or the "powdery sulfur bolete".[3]

Description

Young specimen with an intact partial veil

The cap is rounded to convex before flattening with age, and attains a diameter of 1–10 cm (0.4–3.9 in). Its margin is curved inward when young, and usually has hanging remnants of the partial veil. The surface is dry and initially coated with fine particles, while later it develops fine hairs or small scales that are pressed down flat on the surface; in maturity the surface usually develops fine cracks or wrinkles. It is bright yellow, later turning to orange-red to brownish red. The flesh is white to pale yellow, and, when cut, will slowly stain pale blue, then dingy yellow to pale brown. Its flesh has been described variously as indistinct,[3] or bitter tasting with an odor of hickory leaves.[5] The pore surface is bright yellow before turning dingy yellow to grayish brown with age. It stains greenish blue then grayish brown after being bruised or injured. The pores, which number about 1–3 per millimeter, are angular to almost circular. The tubes comprising the pore surface are 5–8 cm (2.0–3.1 in) deep. The yellow stem measures 4.5–14.5 cm (1.8–5.7 in) long by 0.6–1.6 cm (0.2–0.6 in) thick, and is roughly equal in width throughout or somewhat thicker near the base. It is solid (i.e., not hollow), and, above the level of the base, the surface is covered with minute hairs pressed flat against the surface. The partial veil, also bright yellow, is cottony and powdery, and remains as a ring on the upper portion of the stem,[3] although in some specimens it merges gradually with the stipe surface and becomes inconspicuous.[5] There is white mycelium at the stipe base.[6]

Pulveroboletus ravenelii produces an olive-grey to olive-brown spore print. Spores are elliptical to oval, smooth, and measure 8–10 by 4–5 μm.[3] The hyphal tissue in the hymenophore is inamyloid and bilateral, meaning it diverges downward from the flesh toward the edge of the hymenophore, away from a central strand. The tubes have scattered cystidia on the walls (pleurocystidia) and abundant cystidia on the edges (cheilocystidia). The hyphae in the cap cuticle are arranged as an ixotrichodermium–long and typically multi-celled, with erect hyphae embedded in a gelatinous matrix. Clamp connections are absent from the hyphae.[6]

Habitat and distribution

The fruit bodies of Pulveroboletus ravenelii grow on the ground singly, scattered, or in groups in woods under conifers.[3] Preferred mycorrhizal plant hosts include pine, hemlock, and rhododendron.[5] Fruiting occurs from July to October. In North America, it is distributed from eastern Canada extending south to the Gulf of Mexico, and west to Texas, Michigan, and California.[3] The bolete was reported from a Mexican beech (Fagus mexicana) forest in Hidalgo, Mexico in 2010.[7] It has also been recorded from Costa Rica[8] and Colombia. In Asia, it has been found in Indonesia[6] and China.[9] It has also been recorded from northeast Australia.[6]

Uses

Pulveroboletus ravenelii mushrooms are edible.[3] They have been used in traditional Chinese medicine to treat lumbago, numbed limbs, and as an antihemorrhagic. Bioactive compounds that have been identified from the fruit bodies include pulveravin A, pulveravin B, vulpinic acid,[10] and pulverolide.[11] Mushrooms are also used in mushroom dyeing to produce the colors yellow, gold, greenish yellow, orange, or olive, depending on the mordant used.[12]

See also

References

  1. "Pulveroboletus ravenelii (Berk. & M.A. Curtis) Murrill 1909". MycoBank. International Mycological Association. Retrieved 2013-10-29.
  2. Berkeley MJ, Curtis MA (1853). "Centuries of North American fungi". Annals and Magazine of Natural History. II. 12: 417–35 (see p. 429).
  3. 1 2 3 4 5 6 7 8 Bessette AE, Roody WC, Bessette AR (2000). North American Boletes. Syracuse, New York: Syracuse University Press. pp. 223–4. ISBN 978-0-8156-0588-1.
  4. Murrill WA. (1909). "The Boletaceae of North America – 1". Mycologia. 1 (1): 4–18. doi:10.2307/3753167.
  5. 1 2 3 4 Roody WC. (2003). Mushrooms of West Virginia and the Central Appalachiansb. Lexington, Kentucky: University Press of Kentucky. p. 284. ISBN 978-0-8131-9039-6.
  6. 1 2 3 4 Halling RE, Mueller GM (2005). Common Mushrooms of the Talamanca Mountains, Costa Rica. New York, New York: New York Botanical Garden Press. p. 69. ISBN 978-0-89327-460-3.
  7. Rodríguez-Ramírez EC, Moreno CE (2010). "Bolete diversity in two relict forests of the Mexican beech (Fagus grandifolia var. mexicana; Fagaceae)". American Journal of Botany. 97 (5): 893–898. doi:10.3732/ajb.0900284. PMID 21622453.
  8. Halling RE, Osmundson TW, Neves MA (2008). "Pacific boletes: Implications for biogeographic relationships". Mycological Research. 112 (4): 437–47. doi:10.1016/j.mycres.2007.11.021. PMID 18316181.
  9. Bo L, Bau YS (1980). "Fungi and mycological literature of the Szechwan Province in China". Mycologia. 72 (6): 1117–26. doi:10.2307/3759565. JSTOR 3759565.
  10. Duncan CJ, Cuendet M, Fronczek FR, Pezzuto JM, Mehta RG, Hamann MT, Ross SA (2003). "Chemical and biological investigation of the fungus Pulveroboletus ravenelii". Journal of Natural Products. 66 (1): 103–7. doi:10.1021/np0203990. PMID 12542354.
  11. Yang W, Liu J, Zhang H (2010). "Total synthesis of pulverolide: revision of its structure". Tetrahedron Letters. 51 (37): 4874–76. doi:10.1016/j.tetlet.2010.07.044.
  12. Bessette A, Bessette AR (2001). The Rainbow Beneath my Feet: A Mushroom Dyer's Field Guide. Syracuse, New York: Syracuse University Press. p. 49. ISBN 978-0-8156-0680-2.

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